We have found 46587 results matching your criteria.
Please wait while we search...

General Material Information

Preferred name geraniol
Trivial Name Geraniol
Short Description trans-3,7-dimethyl-2,7-octadien-1-ol
Formula C10 H18 O
CAS Number 106-24-1
Deleted CAS Number 8007-13-4
FEMA Number 2507
ECHA Number 203-377-1
FDA UNII L837108USY
Nikkaji Number J3.240I
Beilstein Number 1722456
MDL MFCD00002917
COE Number 60
xLogP3-AA 2.90 (est)
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 1223 geraniol
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 106-24-1 ; GERANIOL
Synonyms
  • (2E)-3,7-dimethyl-2,6-octadien-1-ol
  • (E)-3,7-dimethyl-2,6-octadien-1-ol
  • 2-trans-3,7-dimethyl-2,6-octadien-1-ol
  • trans-3,7-dimethyl-2,6-octadien-1-ol
  • (2E)-3,7-dimethyl-2,6-octadienol
  • (E)-3,7-dimethyl-2,7-octadien-1-ol
  • trans-3,7-dimethyl-2,7-octadien-1-ol
  • (2E)-3,7-dimethylocta-2,6-dien-1-ol
  • (E)-3,7-dimethylocta-2,6-dien-1-ol
  • beta- geraniol
  • trans- geraniol
  • geraniol (ex palmarosa)
  • geraniol (fine perfumery)
  • geraniol (natural)
  • geraniol #702 (rose base)
  • geraniol 5020
  • geraniol 532
  • geraniol 60
  • geraniol 600
  • geraniol 600 type
  • geraniol 70
  • geraniol 7030
  • geraniol 80
  • geraniol 902
  • geraniol 95 FCC
  • geraniol 950
  • geraniol 96/98 FCC
  • geraniol 98
  • geraniol 98 FCC
  • geraniol 980
  • geraniol 980 pure
  • (E)- geraniol alcohol
  • geraniol BJ
  • geraniol BRI
  • geraniol coeur (IFF)
  • geraniol coeur FCC
  • geraniol crude ex-citronella oil
  • geraniol ex citronella
  • geraniol ex palmarosa
  • geraniol ex palmarosa (natural)
  • geraniol ex palmarosa 98%, natural
  • geraniol ex palmarosa oil
  • geraniol extra
  • geraniol extra 92/94% FCC
  • geraniol finest ex citronella natural
  • geraniol france, natural isolated constituent
  • geraniol india, natural isolated constituent
  • geraniol intermediate 60
  • geraniol natural
  • geraniol natural (ex citronella)
  • geraniol natural ex citronella
  • geraniol natural ex palmarosa
  • geraniol natural from citronella oil
  • geraniol natural from palmarosa oil
  • geraniol natural isolate
  • geraniol perfume grade
  • geraniol prime
  • geraniol standard ex citronella natural
  • geraniol super 96/98% FCC
  • geraniol, natural ex-citronella oil
  • geraniol, natural ex-palmarosa
  • (E)- geranyl alcohol
  • lemonol
  • meranol
  • (E)- nerol
  • (E)- nerol alcohol
  • (E)- neryl alcohol
  • rosoflor
  • (2E)-3,7-dimethylocta-2,6-dien-1-ol
  • 2,6-Octadien-1-ol, 3,7-dimethyl-, (2E)-
  • 2,6-Octadien-1-ol, 3,7-dimethyl-, (E)-
  • (2E)-3,7-Dimethyl-2,6-octadien-1-ol
  • Geranyl alcohol
  • trans-3,7-Dimethyl-2,6-octadien-1-ol
  • trans-Geraniol
  • β-Geraniol
  • (E)-Geraniol
  • (E)-Nerol
  • (E)-3,7-Dimethyl-2,6-octadien-1-ol
  • NSC 9279
  • MosquitoSafe
  • 3,7-Dimethyl-trans-2,6-octadien-1-ol
  • (E)-3,7-Dimethyl-2,6-octadienol
  • trans-1-Hydroxy-3,7-dimethyl-2,6-octadiene
  • TT 4228
  • TT 4302
  • Geraniol super
  • Geraniol Supra
  • ZIF-77
  • Nerol 800

US / EU / FDA / JECFA / FEMA / Scholar / Patents

Google Scholar Start search
Google Books Start search
Google Patents Start search
Perfumer & Flavorists Start search
EU Patents Start search
PubMeb Start search
NCBI Start search

Literature & References

(2E)-3,7-dimethylocta-2,6-dien-1-ol
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:106-24-1
Pubchem (cid):637566
Pubchem (sid):134971627
Flavornet:106-24-1
Pherobase:View
Publications by PubMed
Flavor of cold-hardy grapes: impact of berry maturity and environmental conditions.
Aroma enhancement in wines using co-immobilized Aspergillus niger glycosidases.
Isolation and characterization of terpene synthases potentially involved in flavor development of ripening olive (Olea europaea) fruits.
Evaluation of volatiles from two subtropical strawberry cultivars using GC-olfactometry, GC-MS odor activity values, and sensory analysis.
Characteristic volatile components of Kabosu (Citrus sphaerocarpa Hort. ex Tanaka).
NTP technical report on the toxicology and carcinogenesis studies of beta-myrcene (CAS No. 123-35-3) in F344/N rats and B6C3F1 mice (Gavage studies).
Classification of wines from five Spanish origin denominations by aromatic compound analysis.
Volatile compounds and sensory attributes of wine from Cv. Merlot (Vitis vinifera L.) grown under differential levels of water deficit with or without a kaolin-based, foliar reflectant particle film.
A candidate gene association study on muscat flavor in grapevine (Vitis vinifera L.).
The effects of high hydrostatic pressure treatment on the flavor and color of grated ginger.
Flavor characterization of sugar-added pennywort (Centella asiatica L.) juices treated with ultra-high pressure and thermal processes.
Biotransformation of hop-derived monoterpene alcohols by lager yeast and their contribution to the flavor of hopped beer.
The 1-deoxy-D: -xylulose 5-phosphate synthase gene co-localizes with a major QTL affecting monoterpene content in grapevine.
Comparison of sugar, acids, and volatile composition in raspberry bushy dwarf virus-resistant transgenic raspberries and the wild type 'meeker' (rubus idaeus L.).
Characterization of free flavor compounds in traminette grape and their relationship to vineyard training system and location.
Enrichment of tomato flavor by diversion of the early plastidial terpenoid pathway.
[Study on the pyrolysis behavior of geranyl-beta-D-glucopyranoside by gas chromatography-mass spectrometry].
Characterization of the key aroma compounds in the beverage prepared from Darjeeling black tea: quantitative differences between tea leaves and infusion.
Impact of growing environment on chickasaw blackberry (Rubus L.) aroma evaluated by gas chromatography olfactometry dilution analysis.
Metabolism of geraniol in grape berry mesocarp of Vitis vinifera L. cv. Scheurebe: demonstration of stereoselective reduction, E/Z-isomerization, oxidation and glycosylation.
Lipase-catalyzed production of short-chain acids terpenyl esters of interest to the food industry.
Synthesis of flavor and fragrance esters using Candida antarctica lipase.
Differences in the volatile components and their odor characteristics of green and ripe fruits and dried pericarp of Japanese pepper (Xanthoxylum piperitum DC.).
Crystal structure of amylose complexes with small ligands.
Headspace solid phase microextraction (SPME) analysis of flavor compounds in wines. Effect of the matrix volatile composition in the relative response factors in a wine model.
Downstream processing of enzymatically produced geranyl glucoside.
Acid-catalyzed hydrolysis of alcohols and their beta-D-glucopyranosides.
Purification, characterization, and substrate specificity of a novel highly glucose-tolerant beta-glucosidase from Aspergillus oryzae.
Is there a relationship between odors and motion sickness?
Flowery odor formation revealed by differential expression of monoterpene biosynthetic genes and monoterpene accumulation in rose (Rosa rugosa Thunb.).
Enzymatic modification of palmarosa essential oil: chemical analysis and olfactory evaluation of acylated products.
Assessing the chemotaxis behavior of Physarum polycephalum to a range of simple volatile organic chemicals.
Evaluation of biological and chemical insect repellents and their potential adverse effects.
Characteristic chemical components of the essential oil from white kwao krua (Pueraria mirifica).
Preliminary analysis of several attractants and spatial repellents for the mosquito, Aedes albopictus using an olfactometer.
Solid phase microextraction as a reliable alternative to conventional extraction techniques to evaluate the pattern of hydrolytically released components in Vitis vinifera L. grapes.
Sensory threshold of 1,1,6-trimethyl-1,2-dihydronaphthalene (TDN) and concentrations in young Riesling and non-Riesling wines.
Characterization of volatiles and aroma-active compounds in honeybush (Cyclopia subternata) by GC-MS and GC-O analysis.
Effects of cold immobilization and recovery period on honeybee learning, memory, and responsiveness to sucrose.
Aversive learning overcomes appetitive innate responding in honeybees.
Predication of Japanese green tea (Sen-cha) ranking by volatile profiling using gas chromatography mass spectrometry and multivariate analysis.
Appetitive and aversive learning in Spodoptera littoralis larvae.
Terpene down-regulation in orange reveals the role of fruit aromas in mediating interactions with insect herbivores and pathogens.
An artificial neural network approach for glomerular activity pattern prediction using the graph kernel method and the gaussian mixture functions.
Evolution of aroma and phenolic compounds during ripening of 'superior seedless' grapes.
Aroma character impact compounds in Kinokuni mandarin orange (Citrus kinokuni) compared with Satsuma mandarin orange (Citrus unshiu).
Recruits of the stingless bee Scaptotrigona pectoralis learn food odors from the nest atmosphere.
Aroma constituents and alkylamides of red and green huajiao (Zanthoxylum bungeanum and Zanthoxylum schinifolium).
Performance of mice in discrimination of liquor odors: behavioral evidence for olfactory attention.
Characterization of the most odor-active volatiles of orange wine made from a Turkish cv. Kozan (Citrus sinensis L. Osbeck).
Comparison of odor-active compounds in the spicy fraction of hop (Humulus lupulus L.) essential oil from four different varieties.
Syntheses and odor descriptions of cyclopropanated compounds, part 6: Analogs of aliphatic monoterpene dienols and non-branched alcohols.
Comparison of the odor-active compounds in unhopped beer and beers hopped with different hop varieties.
Foot odor due to microbial metabolism and its control.
Restrained eaters show altered brain response to food odor.
Maturation of odor representation in the honeybee antennal lobe.
Olfactory blocking and odorant similarity in the honeybee.
Role of suggestion in odor-induced mood change.
Sensory and instrumental evaluation of catnip (Nepeta cataria L.) aroma.
Tonic and phasic receptor neurons in the vertebrate olfactory epithelium.
Behavioral and electrophysiological responses of natural enemies to synomones from tea shoots and kairomones from tea aphids, Toxoptera aurantii.
Non-specific olfactory aversion induced by intrabulbar infusion of the GABA(A) receptor antagonist bicuculline in young rats.
Geraniol dehydrogenase activity related to aroma formation in ginger (Zingiber officinale Roscoe).
Blocking and the detection of odor components in blends.
Odor suppression of voltage-gated currents contributes to the odor-induced response in olfactory neurons.
The main citral-geraniol and carvacrol chemotypes of the essential oil of thymus pulegioides L. growing wild in vilnius district (Lithuania).
Similarities in the aroma chemistry of Gewürztraminer variety wines and lychee (Litchi chinesis sonn.) fruit.
Sensory properties of selected terpenes. Thresholds for odor, nasal pungency, nasal localization, and eye irritation.
Analysis of interaction in binary odorant mixtures.
Trigeminal and olfactory chemosensory impact of selected terpenes.
Learning in the Africanized honey bee: Apis mellifera L.
Odor discrimination of "IP3-" and "cAMP-increasing" odorants in the turtle olfactory bulb.
Comparison of models of odor interaction.
Olfactory sensitivity to the pheromone, androstenone, is sexually dimorphic in the pig.
The nature and course of olfactory deficits in Alzheimer's disease.
Evaluation of antifungal volatile compounds on the basis of the elongation rate of a single hypha.
Detection of propionic acid vapor by rats with lesions of olfactory bulb areas associated with high 2-DG uptake.
Olfactory responses of a specialist and a generalist grasshopper to volatiles ofArtemisia ludoviciana nutt. (Asteraceae).
Odor mimetism? : Key substances inOphrys lutea-Andrena pollination relationship (Orchidaceae: Andrenidae).
Reactions of olfactory bulb neurons to different stimulus intensities in laboratory mice.
Olfactory deprivation enhances normal spine loss in the olfactory bulb of developing ferrets.
The influence of permanent odor stimuli on the postnatal development of neural activity in the olfactory bulbs of laboratory mice.
The Nasonov pheromone of the honeybeeApis mellifera L. (Hymenoptera, Apidae). Part II. Bioassay of the components using foragers.
Specific anosmia to geraniol in mice.
Slow potentials of the turtle olfactory bulb in response to odor stimulation of the nose.
Publications by J-Stage
The Effects of High Hydrostatic Pressure Treatment on the Flavor and Color of Grated Ginger
Characteristic chemical components of the essential oil from white kwao krua (Pueraria mirifica)
Aroma Character Impact Compounds in Kinokuni Mandarin Orange (Citrus kinokuni) Compared with Satsuma Mandarin Orange (Citrus unshiu)

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
UM BBD:Search
KEGG (GenomeNet):C01500
HMDB (The Human Metabolome Database):HMDB35155
FooDB:FDB013792
YMDB (Yeast Metabolome Database):YMDB01700
Export Tariff Code:2905.22.5050
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
Formulations/Preparations:
hercon japanese beetle food lure; active ingredient 9.84% 2-phenylethyl propionate, 23.0% eugenol, 4.84% geraniol lure n kill japanese beetle; active ingredient 9.84% 2-phenylethyl propionate, 23.0% eugenol, 0.47% (r,z)-5-(1-decenyl)dihydro-2(3h)-furanone, 9.84% geraniol bag-a-bug japanese beetle trap; active ingredient 0.84% 2-phenylethyl propionate, 23.0% eugenol, 0.47% (r,z)-5-(1-decenyl)dihydro-2(3h)-furanone, 2.84% geraniol japanese beetle combo bait; active ingredient 9.43% 2-phenylethyl propionate, 21.98& eugenol, 0.02% (r,z)-5-(1-decenyl)dihydro-2(3h)-furanone, 9.43% geraniol japanese beetle bait ii; active ingredient 9.50% 2-phenylethyl propionate, 22.25% eugenol, 0.133% (r,z)-5-(1-decenyl)dihydro-2(3h)-furanone, 9.50% geraniol trece japanese beetle trap; active ingredient 9.50% 2-phenylethyl propionate, 22.25% eugenol, 0.133% (r,z)-5-(1-decenyl)dihydro-2(3h)-furanone, 9.50% geraniol surefire japanese beetle trap; active ingredient 10.698% 2-phenylethyl propionate, 25.233% eugenol, 0.017% (r,z)-5-(1-decenyl)dihydro-2(3h)-furanone, 10.698% geraniol scent-off twist-ons and scent-off pellets; active ingredient 0.20% allyl isothiocyanate, 1.20% oil of citronella, 2.00% oil of lemongrass, 0.02% oil of orange, 0.02% methyl salicylate, 0.11% bergamot oil, 0.01% alpha-ionone, 0.04% geraniol biomite; active ingredient 0.167% farnesol, 0.417% nerolidol, 0.417% 3,7-dimethyl-6-octen-1-ol, 0.417% geraniol grade: standard; soap; synthetic; fcc; eoa. commercial product contains 88% minimum geraniol. ester content is not more than 1% (as geranyl acetate). aldehyde content is not more than 1% (as citronellol). from table

Suppliers

Advanced Biotech Alfa Biotechnology
Alfrebro Ambles Nature et Chimie
Argeville Aromatic and Allied Chemicals
Arora Aromatics Associate Allied Chemicals
Augustus Oils Aurochemicals
Axxence Aromatic Azelis UK
BASF Bedoukian Research
Beijing Lys Chemicals Berjé
BOC Sciences Charkit Chemical
Citrus and Allied Essences CJ Latta & Associates
Coompo Creatingperfume.com
De Monchy Aromatics Diffusions Aromatiques
DRT Terpenes ECSA Chemicals
Elan Inc. Ernesto Ventós
Excellentia International ExtraSynthese
Fine Fragrances Pvt Ltd Fleurchem
Foreverest Resources Fuzhou Farwell
Gem Aromatics Global Essence
HDDES Group Hermitage Oils
IFF Indenta Group
Indukern F&F Jiangyin Healthway
K.L. Koh Enterprise Keva
Kun Shan P&A Lluch Essence
M&U International Moellhausen
Nagar Haveli Perfumes & Aromatics Naturamole
OQEMA Payand Betrand
Pearlchem Corporation Pell Wall Perfumes
Penta International PerfumersWorld
Perfumery Laboratory Phoenix Aromas & Essential Oils
Prodasynth Quimdis
R C Treatt & Co Ltd Reincke & Fichtner
Robertet Santa Cruz Biotechnology
Sigma-Aldrich Silverline Chemicals
Som Extracts SRS Aromatics
Symrise Synerzine
Takasago Taytonn ASCC
TCI AMERICA Tengzhou Xiang Yuan Aroma Chemicals
The Good Scents Company The John D. Walsh Company
The Lermond Company The Perfumers Apprentice
Ungerer & Company Van Aroma
Vigon International WEN International
Xiamen Doingcom Chemical Zanos
Advanced Biotech. Inc. Alfrebro LLC/ Archer Daniels Midland Company
Argeville SAS Augustus Oils Ltd
Axxence Aromatic GmbH Azelis UK Ltd.
Bedoukian Research, Inc. Beijing Lys Chemicals Co, LTD.
Berje Inc. Charkit Chemical Corporation
CJ Latta & Associates, LLC Fleurchem, Inc.
Foreverest Resources Ltd. Global Essence Inc.
Hermitage Oils / Neroli S.R.L. Indukern, S.A. F&F Ingredients Division
Jiangyin Healthway International Trade Co., Ltd Lluch Essence S.L.
M&U International LLC Moellhausen S.P.A.
Penta International Corporation PerfumersWorld Ltd.
Robertet, Inc. SRS Aromatics Ltd
Symrise AG Synerzine, Inc.
Taytonn ASCC Pte Ltd The John D. Walsh Company, Inc
R C Treatt and Co Ltd Ernesto Ventós S.A.
Zanos Ltd.

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 154.2526550293
Specific gravity @ 25 °C
Pounds per Gallon 7.239 to 7.364
Specific gravity @ 20 °C
Pounds per Gallon 7.231 to 7.298
Refractive Index 1.469 to 1.482 @ 20 °C
Melting Point -16 to -14°C @ 760 mm Hg
Boiling Point 229 to 230°C @ 760 mm Hg
Boiling Point 111 to 112°C @ 10 mm Hg
Acid Value 1 max KOH/g
Vapor Pressure 0.021 mmHg @ 25 °C
Vapor Density 5.31
Flash Point TCC Value 108 °C TCC
logP (o/w) 3.56
Shelf life 24 months (or longer if stored properly.)
Storage notes Store in cool, dry place in tightly sealed containers, protected from heat and light.
Solubility
alcohol Yes
fixed oils Yes
kerosene Yes
paraffin oil Yes
propylene glycol Yes
water, 100 mg/L @ 25 °C (exp) Yes
glycerin No
Stability
alcoholic lotion Unspecified
antiperspirant Unspecified
deo stick Unspecified
detergent perborate Unspecified
fabric softener Unspecified
hair spray Unspecified
hard surface cleaner Unspecified
non-discoloring in most media Unspecified
shampoo Unspecified
soap Unspecified

Organoleptic Properties

Odor Type: Floral
sweet, floral, fruity, rose, waxy, citrus, citronella
Odor strength medium
Substantivity 60 hour(s) at 100.00 %
Luebke, William tgsc, (1981) At 100.00 %. sweet floral fruity rose waxy citrus
Mosciano, Gerard P&F 22, No. 6, 41, (1997) At 2.00 %. Floral, sweet, rosey, fruity and citronella-like with a citrus nuance
Flavor Type: Floral
floral, rose, waxy, fruity, peach
Mosciano, Gerard P&F 22, No. 6, 41, (1997) At 3.00 ppm. Floral, rosy, waxy and perfumey with a fruity, peach-like nuance
Used in many flavors such as cherry, peach, raspberry, grapefruit, red apple, plum, lime, orange, lemon, watermelon, pineapple and blueberry flavors. Floral

Occurrences

Potential Uses

Applications
Odor purposes Acacia, Aldehydic, Almond, Amber, Apple, Apple red apple, Apricot, Azalea, Baby powder, Berry, Blackberry, Blue grass, Blueberry, Bois de rose, Botanical, Bouquet, Boysenberry, Butterscotch, Carnation, Cassia, Castoreum, Cedarwood, Champaca, Cherry, Cherry blossom, Cinnamon, Citronella, Clary sage oil replacer, Clover, Coconut tropical coconut, Cologne, Coriander, Country meadow, Crabapple blossom, Dill weed, Eucalyptus oil replacer, Fagonia, Fern, Floral, Geranium, Gingergrass, Grapefruit, Green, Hawthorn, Heliotrope, Hibiscus, Honey, Honeysuckle, Hyacinth, Jasmin, Lavandin, Lavender, Lavender spike lavender, Lemon, Lemongrass, Lilac, Lily, Lily of the valley, Lime, Linaloe wood, Linden flower, Mace, Magnolia, Mandarin, Melon, Mimosa, Moss, Myrrh, Myrtle oil replacer, Narcissus, Neroli, Nutmeg, Orange, Orange blossom, Orchid, Orris, Palmarosa oil replacer, Peach, Pear, Peony, Floral, Petitgrain bergamot petitgrain, Petitgrain lemon petitgrain, Pineapple, Plum, Poppy red poppy, Powder, Rain, Raspberry, Rose, Rose absolute replacer, Rose d'orient, Rose moss rose, Rose red rose, Rose tea rose, Rose white rose, Sandalwood, Sassafras, Savin, Sherry, Snake root, Strawberry, Sweet pea, Thyme oil white replacer, Tuberose, Vanilla, Verbena, Violet, Wallflower, Wine, Ylang ylang, Zibeline
Flavoring purposes Beer, Carrot, Coriander, Dill weed, Fruit punch, Lavender spike lavender, Linaloe wood, Petitgrain bergamot petitgrain, Petitgrain lemon petitgrain, Savin, Snake root, Tea black tea, Tea black tea
Other purposes Chanel #5, Erica, Jicky, My sin
Cosmetic purposes Perfuming agents, Tonic

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and eyes.
R 41 - Risk of serious damage to eyes.
R 43 - May cause sensitisation by skin contact.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Skin irritation (Category 2), H315
Skin sensitisation (Category 1), H317
Acute aquatic toxicity (Category 3), H402
GHS Label elements, including precautionary statements
Pictogramcorrosion.jpgexclamation-mark.jpg
Signal word Danger
Hazard statement(s)
H315 - Causes skin irritation
H317 - May cause an allergic skin reaction
H318 - Causes serious eye damage
H402 - Harmful to aquatic life
Precautionary statement(s)
P261 - Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 - Wash skin thouroughly after handling.
P272 - Contaminated work clothing should not be allowed out of the workplace.
P273 - Avoid release to the environment.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P302 + P352 - IF ON SKIN: wash with plenty of soap and water.
P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P310 - Immediately call a POISON CENTER or doctor/physician.
P321 - Specific treatment (see supplemental first aid instructions on this label).
P333 + P313 - IF SKIN irritation or rash occurs: Get medical advice/attention.
P362 - Take off contaminated clothing and wash before reuse.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Human Experience:
6 % solution: no sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50 3600 mg/kg
SKIN AND APPENDAGES (SKIN): HAIR: OTHER BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: COMA
Food and Cosmetics Toxicology. Vol. 2, Pg. 327, 1964.

intramuscular-mouse LD50 4000 mg/kg
Journal of Scientific and Industrial Research, Section C: Biological Sciences. Vol. 21, Pg. 342, 1962.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 12, Pg. 881, 1974.

subcutaneous-mouse LD50 1090 mg/kg
PERIPHERAL NERVE AND SENSATION: SPASTIC PARALYSIS WITH OR WITHOUT SENSORY CHANGE
Sapporo Igaku Zasshi. Sapporo Medical Journal. Vol. 3, Pg. 73, 1952.

Inhalation Toxicity:
Not determined

Safety in use information

Category:
flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
IFRA Critical Effect:
Dermal sensitization
View the IFRA Standard
View IFRA Standards Library for complete information.
Please review Amendment 49 IFRA documentation for complete information.
IFRA RESTRICTION LIMITS IN THE FINISHED PRODUCT (%):
Category 1: Products applied to the lips
0.85 %
Category 2: Products applied to the axillae
0.25 %
Category 3: Products applied to the face/body using fingertips
5.10 %
Category 4: Products related to fine fragrance
4.70 %
Category 5: Products applied to the face and body using the hands (palms), primarily leave-on
Category 5A: Body lotion products applied to the body using the hands (palms), primarily leave-on
1.20 %
Category 5B: Face moisturizer products applied to the face using the hands (palms), primarily leave-on
1.20 %
Category 5C: Hand cream products applied to the hands using the hands (palms), primarily leave-on
1.20 %
Category 5D: Baby Creams, baby Oils and baby talc
1.20 %
Category 6: Products with oral and lip exposure
2.80 %
Category 7: Products applied to the hair with some hand contact
Category 7A: Rinse-off products applied to the hair with some hand contact
9.60 %
Category 7B: Leave-on products applied to the hair with some hand contact
9.60 %
Category 8: Products with significant anogenital exposure
0.50 %
Category 9: Products with body and hand exposure, primarily rinse off
9.20 %
Category 10: Household care products with mostly hand contact
Category 10A: Household care excluding aerosol products (excluding aerosol/spray products)
33.00 %
Category 10B: Household aerosol/spray products
33.00 %
Category 11: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate
Category 11A: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate without UV exposure
18.00 %
Category 11B: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate with potential UV exposure
18.00 %
Category 12: Products not intended for direct skin contact, minimal or insignificant transfer to skin
No Restriction
Notes:
IFRA FLAVOR REQUIREMENTS:

Due to the possible ingestion of small amounts of fragrance ingredients from their use in products in Categories 1 and 6, materials must not only comply with IFRA Standards but must also be recognized as safe as a flavoring ingredient as defined by the IOFI Code of Practice (www.iofi.org). For more details see chapter 1 of the Guidance for the use of IFRA Standards.

Maximised Survey-derived Daily Intakes (MSDI-EU): 550.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 315.00 (μg/capita/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3
Click here to view publication 3
average usual ppmaverage maximum ppm
baked goods: -11.00000
beverages(nonalcoholic): -2.10000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: 0.800002.90000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -3.30000
fruit ices: -3.30000
gelatins / puddings: 2.000002.00000
granulated sugar: --
gravies: --
hard candy: -10.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --

Safety references

European Food Safety Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...

European Food Safety Authority (EFSA) reference(s):

Flavouring Group Evaluation 202: 3-Alkylated aliphatic acyclic alpha,beta-unsaturated aldehydes and precursors with or without additional double bonds from chemical subgroup 1.1.3 of FGE.19[1]
View page or View pdf

Flavouring Group Evaluation 72 (FGE.72): Consideration of aliphatic, branched-chain saturated and unsaturated alcohols, aldehydes, acids, and related esters evaluated by the JECFA (61st meeting) structurally related to branched- and straight-chain unsaturated carboxylic acids. Esters of these and straight-chain aliphatic saturated alcohols evaluated by EFSA in FGE.05Rev2 (2010)
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 95 (FGE.95): Consideration of aliphatic, linear or branched-chain saturated and unsaturated alcohols, aldehydes, acids and related esters evaluated by JECFA (69th meeting) structurally related to esters of branched- and straight-chain aliphatic saturated primary alcohols and of one secondary alcohol, and branched- and straight-chain unsaturated carboxylic acids evaluated by EFSA in FGE.05Rev1 (2008)
View page or View pdf

Conclusion on the peer review of the pesticide risk assessment of the active substance geraniol
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 72, Revision 1 (FGE.72Rev1): Consideration of aliphatic, branched-chain saturated and unsaturated alcohols, aldehydes, acids, and related esters evaluated by the JECFA (61st meeting) structurally related to branched- and straight-chain unsaturated carboxylic acids, esters of these and straight-chain aliphatic saturated alcohols evaluated by EFSA in FGE.05Rev2
View page or View pdf

Safety and efficacy of a,ß-unsaturated straight-chain and branched-chain aliphatic primary alcohols, aldehydes, acids and esters belonging to chemical group 3 when used as flavourings for all animal species
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 72, Revision 2 (FGE.72Rev2): consideration of aliphatic, branched-chain saturated and unsaturated alcohols, aldehydes, acids and related esters evaluated by JECFA (61st, 68th and 69th meetings) and structurally related to flavouring substances in FGE.05Rev3
View page or View pdf

EPI System: View
Daily Med:search
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):106-24-1
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :637566
National Institute of Allergy and Infectious Diseases:Data
SCCNFP:opinion
WGK Germany:1
(2E)-3,7-dimethylocta-2,6-dien-1-ol
Chemidplus:0000106241
EPA/NOAA CAMEO:hazardous materials
RTECS:RG5830000 for cas# 106-24-1